Have questions? Visit https://www.reddit.com/r/SNPedia

rs11676348

From SNPedia

Orientationplus
Stabilizedplus
Make rs11676348(C;C)
Make rs11676348(C;T)
Make rs11676348(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position218145423
is asnp
is mentioned by
dbSNPrs11676348
ebirs11676348
HLIrs11676348
Exacrs11676348
Varsomers11676348
Maprs11676348
PheGenIrs11676348
hapmaprs11676348
1000 genomesrs11676348
hgdprs11676348
ensemblrs11676348
gopubmedrs11676348
geneviewrs11676348
scholarrs11676348
googlers11676348
pharmgkbrs11676348
gwascentralrs11676348
openSNPrs11676348
23andMers11676348
23andMe allrs11676348
SNP Nexus

SNPshotrs11676348
SNPdbers11676348
MSV3drs11676348
GWAS Ctlgrs11676348
GMAF0.4568
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21297633OA-icon.png]
Trait
Title Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Risk Allele T
P-val 1E-10
Odds Ratio 1.0700 [1.03-1.11]


[PMID 26071399] Identification of a Common Variant with Potential Pleiotropic Effect on Risk of Inflammatory Bowel Disease and Colorectal Cancer